Canonical Allele Identifier: PA213855
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36259
ClinVar RCV Id: RCV000029922 RCV002463612
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Leu271Pro
CA213854
NM_000162.5:c.812T>C